Eur Rev Med Pharmacol Sci 2014; 18 (17): 2482-2490

Identifying significant crosstalk of pathways in tuberous sclerosis complex

B.-L. Zhang, L.-J. Wang, L. Sun, H.-L. Zhang, X.-M. Wu, Y. Sun, F. Deng, Y. Zhang, Y.-Y. Cheng, J.-C. Feng

Department of Neurology, the First Hospital of Jilin University, Changchun, China. ceiceiliazbl@163.com


OBJECTIVE: Tuberous sclerosis complex (TSC) is the second most common phakomatosis and is characterized by the formation of benign hamartomas and low-grade neoplasms in multiple organ systems. In this study, our objective here was to explore the interaction and crosstalk between pathways in response to tuberous sclerosis complex.

MATERIALS AND METHODS: We enriched the significant pathways and made the crosstalk analysis of the significant pathways.

RESULTS: The results showed that ECM-receptor interaction was a significant pathway in TSC. In addition, insulin-signaling and mTOR signaling also have been identified involved in TSC here, which have been well characterized. Further analysis indicated that there was a crosstalk between ECM-receptor interaction and antigen processing and presentation, ECM-receptor interaction and apoptosis, and leishmaniasis-oxidative phosphorylation-pancreatic cancer. In this study, a network-based approach was used to analyze the crosstalk among TSC related pathways. The crosstalk of pathways is found and analyzed using the PPI datasets and expression profiles.

CONCLUSIONS: Our work showed that comprehensive and system-wide analysis could provide evidence for TSC pathway and complement the traditional component-based approaches. The crosstalk identified might provide new alternative insights into the TSC pathology, which may contribute to the development of novel therapeutic targets for TSC.

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To cite this article

B.-L. Zhang, L.-J. Wang, L. Sun, H.-L. Zhang, X.-M. Wu, Y. Sun, F. Deng, Y. Zhang, Y.-Y. Cheng, J.-C. Feng
Identifying significant crosstalk of pathways in tuberous sclerosis complex

Eur Rev Med Pharmacol Sci
Year: 2014
Vol. 18 - N. 17
Pages: 2482-2490